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LOXL3
Lysyl oxidase like 3This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016]
Top validated antibodies |
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| LSBio |  LS-C165846 |
Polyclonal |
WB
IHC
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| antibodies-online | ABIN953203 |
2 references | Polyclonal |
WB
IHC
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| NSJ Bioreagents | F42503 |
Polyclonal |
WB
EL
IHC
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| Novus Biologicals | H00084695-A01 |
1 references | Polyclonal |
WB
EL
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| NovoPro Bioscience Inc. | 118145 |
Polyclonal |
WB
EL
IHC
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